Onebridge

Regulatory Content Writer, Pharma

Onebridge

full-time

Posted on:

Location: 🇺🇸 United States

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Job Level

Mid-LevelSenior

Tech Stack

AEM

About the role

  • Write and edit patient-friendly content for clinical trial web pages, including trial summaries, study duration, inclusion/exclusion criteria, and other key details, using trial protocols as source material.
  • Ensure content meets health literacy standards, is easily translatable for global audiences, and supports accessibility across reading levels and cognitive abilities.
  • Collaborate with UX, web development, and design teams to align content with user experience goals and contribute to system migrations (e.g., from Contentful to Adobe Experience Manager).
  • Expand and update content across research area pages (e.g., oncology, neuroscience, diabetes) and broader website sections.
  • Support executive communication needs by simplifying complex medical and business information into clear, visual, and engaging presentations.
  • Support graphic design needs for digital or print assets, especially in collaboration with global or capacity-constrained teams.

Requirements

  • 5+ years of experience in content writing, health communication, or a related role, preferably in the pharmaceutical or healthcare industry.
  • Proven ability to interpret clinical trial protocols and summarize medical information in clear, patient-friendly language.
  • Familiarity with global IRB/ERB requirements, international regulatory considerations, and web-based clinical trial recruitment practices.
  • Strong understanding of SEO best practices for healthcare content and writing for global, multilingual audiences.
  • Experience with Adobe Experience Manager (AEM) or similar CMS platforms; familiarity with Contentful and Copilot tools is a plus.
  • Proficiency with Adobe Creative Suite (Illustrator, InDesign, Photoshop, Premiere Pro, AfterEffects) and Microsoft PowerPoint; ability to visualize and simplify information is a plus.
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